NUVASIVE MAXCESS LIGHT GUIDE

NUVASIVE MAXCESS LIGHT GUIDE is an FDA 510(k)-cleared medical device (K042034) manufactured by Nuvasive, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 25, 2004. Regulation: 8.